Key Responsibilities

• Lead the development and execution of the medical affairs strategy for assigned therapeutic areas and assets.
• Co-develop integrated evidence plans, including interventional and non-interventional studies, real-world evidence (RWE), and implementation science.
• Collaborate with Medical Science Liaisons (MSLs), Field Medical teams, and external stakeholders to deliver high-impact medical education and scientific communication.
• Represent GMA in cross-functional forums, including regulatory, commercial, and development teams.
• Provide strategic input into reimbursement and market access strategies.
• Ensure compliance with internal policies and external regulatory standards.
• Act as a subject matter expert and provide leadership in complex scientific and regulatory environments.

Requirements

• MD (preferred), PhD, or PharmD in Health Sciences.
• Several years of experience in Medical Affairs and/or Clinical Development within the pharmaceutical industry.
• Proven ability to lead cross-functional teams and influence stakeholders in a matrix organization.
• Strong understanding of healthcare systems, regulatory environments, and external stakeholder dynamics.
• Excellent communication, strategic thinking, and problem-solving skills.
• Fluent in English (written and spoken

Commitment to Diversity & Inclusion:  

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.